Canonical Allele Identifier: CA1752721652

Gene: PRKAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151565729C= , CM000669.2:g.151565729C=	GRCh38
NC_000007.13:g.151262815C= , CM000669.1:g.151262815C=	GRCh37
NC_000007.12:g.150893748C=	NCBI36
NG_007486.1:g.316502G=
NG_007486.2:g.316503G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478989.7:c.*126G=	ENSP00000420645.3:n.*126G=
ENST00000652321.2:c.1387G=	ENSP00000498886.2:p.Asp463=
ENST00000287878.9:c.1390G= MANE Select	ENSP00000287878.3:p.Asp464=
ENST00000476632.2:c.667G=	ENSP00000419493.2:p.Asp223=
ENST00000478989.6:c.491G=
ENST00000492843.6:c.1015G=	ENSP00000419577.2:p.Asp339=
ENST00000650851.1:n.884G=
ENST00000650858.1:c.607G=	ENSP00000498384.1:p.Asp203=
ENST00000650948.1:n.2319G=
ENST00000651188.1:c.*503G=	ENSP00000498557.1:n.*503G=
ENST00000651303.1:c.*709G=	ENSP00000498428.1:n.*709G=
ENST00000651378.1:c.667G=	ENSP00000499103.1:p.Asp223=
ENST00000651764.1:c.1258G=	ENSP00000498796.1:p.Asp420=
ENST00000651836.1:c.1244G=	ENSP00000499156.1:n.1244G=
ENST00000651954.1:n.1606G=
ENST00000652047.1:c.1255G=	ENSP00000499111.1:p.Asp419=
ENST00000652136.1:n.1937G=
ENST00000652159.1:c.1258G=	ENSP00000499025.1:p.Asp420=
ENST00000652397.1:c.*126G=	ENSP00000498351.1:n.*126G=
ENST00000287878.8:c.1390G=	ENSP00000287878.3:p.Asp464=
ENST00000392801.6:c.1258G=	ENSP00000376549.2:p.Asp420=
ENST00000418337.6:c.667G=	ENSP00000387386.2:p.Asp223=
ENST00000478989.5:c.*126G=	ENSP00000420645.1:n.*126G=
ENST00000492843.5:c.1018G=	ENSP00000419577.1:p.Asp340=
NM_001040633.1:c.1258G=	NP_001035723.1:p.Asp420=
NM_001304527.1:c.1015G=	NP_001291456.1:p.Asp339=
NM_001304531.1:c.667G=	NP_001291460.1:p.Asp223=
NM_016203.3:c.1390G=	NP_057287.2:p.Asp464=
NM_024429.1:c.667G=	NP_077747.1:p.Asp223=
XM_005250002.2:c.1390G=	XP_005250059.1:p.Asp464=
XM_005250004.2:c.1258G=	XP_005250061.1:p.Asp420=
XM_005250006.3:c.1018G=	XP_005250063.1:p.Asp340=
XM_006716021.2:c.1378G=	XP_006716084.1:p.Asp460=
XM_011516282.1:c.1375G=	XP_011514584.1:p.Asp459=
XM_011516283.1:c.1378G=	XP_011514585.1:p.Asp460=
XM_011516284.1:c.1375G=	XP_011514586.1:p.Asp459=
XM_011516285.1:c.667G=	XP_011514587.1:p.Asp223=
XM_011516286.1:c.643G=	XP_011514588.1:p.Asp215=
XM_011516287.1:c.607G=	XP_011514589.1:p.Asp203=
NM_001363698.1:c.1018G=	NP_001350627.1:p.Asp340=
XM_005250002.4:c.1390G=	XP_005250059.1:p.Asp464=
XM_005250004.4:c.1258G=	XP_005250061.1:p.Asp420=
XM_005250006.5:c.1018G=	XP_005250063.1:p.Asp340=
XM_011516285.2:c.667G=	XP_011514587.1:p.Asp223=
XM_011516286.2:c.643G=	XP_011514588.1:p.Asp215=
XM_017012268.2:c.1255G=	XP_016867757.1:p.Asp419=
XM_017012269.1:c.1387G=	XP_016867758.1:p.Asp463=
XM_017012270.1:c.1258G=	XP_016867759.1:p.Asp420=
XM_017012271.2:c.1255G=	XP_016867760.1:p.Asp419=
XM_017012272.1:c.1255G=	XP_016867761.1:p.Asp419=
XM_017012274.2:c.664G=	XP_016867763.1:p.Asp222=
XM_017012275.2:c.607G=	XP_016867764.1:p.Asp203=
XM_017012276.2:c.664G=	XP_016867765.1:p.Asp222=
XM_017012277.2:c.643G=	XP_016867766.1:p.Asp215=
XM_017012278.1:c.607G=	XP_016867767.1:p.Asp203=
XM_017012279.2:c.607G=	XP_016867768.1:p.Asp203=
XM_017012280.2:c.607G=	XP_016867769.1:p.Asp203=
XM_017012281.2:c.607G=	XP_016867770.1:p.Asp203=
XM_024446786.1:c.1258G=	XP_024302554.1:p.Asp420=
XM_024446787.1:c.667G=	XP_024302555.1:p.Asp223=
XM_024446788.1:c.664G=	XP_024302556.1:p.Asp222=
XM_024446789.1:c.667G=	XP_024302557.1:p.Asp223=
NM_016203.4:c.1390G= MANE Select	NP_057287.2:p.Asp464=
NM_001040633.2:c.1258G=	NP_001035723.1:p.Asp420=
NM_001304527.2:c.1015G=	NP_001291456.1:p.Asp339=
NM_001304531.2:c.667G=	NP_001291460.1:p.Asp223=
NM_001363698.2:c.1018G=	NP_001350627.1:p.Asp340=
NM_024429.2:c.667G=	NP_077747.1:p.Asp223=